SCHEMBL11209484

SCHEMBL11209484

CC(C)(C)c1ccc(C(Cl)(Cl)Cl)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.55
LMNA P02545 1/20 0.52
TYR P14679 1/20 0.52
KIF11 P52732 2/20 0.44
ALDH1A1 P00352 5/20 0.42
HSD11B1 P28845 1/20 0.42
HPGD P15428 2/20 0.41
NPC1 O15118 2/20 0.41
RAB9A P51151 2/20 0.41
MAPT P10636 1/20 0.41
MAPK1 P28482 1/20 0.41
HDAC1 Q13547 1/20 0.41
SLC22A2 O15244 1/20 0.41
SLC22A1 O15245 1/20 0.41
SLC22A3 O75751 1/20 0.41
BCHE P06276 3/20 0.40
ACHE P22303 3/20 0.40
ALOX15 P16050 1/20 0.40
HSD17B10 Q99714 1/20 0.40
TDP1 Q9NUW8 1/20 0.40

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL424728 0.83 TSHR (0.73) TSHRLMNATYRKIF11ALDH1A1
SCHEMBL545084 0.83 TSHR (0.67) TSHRLMNAMAPK1TDP1
SCHEMBL9816151 0.83 TSHR (0.67) TSHRLMNAMAPK1TDP1
SCHEMBL13704994 0.81 TSHR (0.55) TSHRLMNATYRKIF11ALDH1A1
SCHEMBL11551232 0.81 TSHR (0.52) TSHRLMNATYRALDH1A1HPGD
SCHEMBL7565907 0.81 TSHR (0.55) TSHRLMNATYRKIF11ALDH1A1
SCHEMBL18242376 0.77 TSHR (0.46) TSHRLMNATYRALDH1A1HSD11B1
Hydrogen Peroxide SCHEMBL28677809 0.76 LMNA (0.71) TSHRLMNATYRKIF11ALDH1A1
SCHEMBL1538589 0.75 TSHR (0.55) TSHRLMNAALDH1A1HPGDNPC1
SCHEMBL8889645 0.75 TSHR (0.55) TSHRLMNATYRKIF11ALDH1A1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0045425-B1 PROCESS FOR THE HALOGENATION OF POSSIBLY SUBSTITUTED 4-TERT.-BUTYL TOLUENES AND THE MIXTURES OBTAINED THEREFROM OF POSSIBLY SUBSTITUTED 4-TERT.-BUTYLBENZAL HALOGENIDES, 4-TERT.-BUTYLBENZYL HALOGENIDES AND 4-TERT.-BUTYLBENZO TRIHALOGENIDES BAYER AG (DE) 1983-11-23 EP disclosed
US-4306102-A CHEMICAL INTERMEDIATES IN THE FORMATION OF P-TERT-BUTYL BENZOIC ACID HOECHST AKTIENGESELLSCHAFT (DE) 1981-12-15 US disclosed
EP-0011288-A1 p-Tert.-butylbenzotribromide and his derivatives which are substituted in the ring by halogen, a process for their preparation as well as their use. HOECHST AKTIENGESELLSCHAFT (DE) 1980-05-28 EP disclosed
US-4163753-A FROM AN ALIPHATIC ACID ANHYDRIDE AND A TRICHLOROMETHYL AROMATIC COMPOUND Diaz Chemical Corporation (US) 1979-08-07 US disclosed